Source: GENOMICS_ENGLAND

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
FANCONI ANEMIA, COMPLEMENTATION GROUP O
disease 0.710 moderate 1.000 5 0 2003 2018
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3
disease 0.700 None 1.000 2 0 2003 2017
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
disease 0.700 strong 0.947 0 0 2010 2020
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia
disease 0.600 moderate 1.000 4 0 2009 2019
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
group 0.400 moderate 1.000 1 0 2017 2017
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C0265219
Disease: Miller Dieker syndrome
Miller Dieker syndrome
disease 0.300 moderate 1.000 1 0 2017 2017
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C0030312
Disease: Pancytopenia
Pancytopenia
disease 0.300 moderate 1.000 1 0 2017 2017
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity
phenotype 0.300 moderate 1.000 1 0 2017 2017
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
disease 0.300 moderate 1.000 1 0 2017 2017
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
disease 0.300 moderate 1.000 1 0 2017 2017
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
RAD51 paralog C 0.533 0.692 6.2E-14
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray
phenotype 0.300 moderate 1.000 1 0 2018 2018